Cheng Chialin, Fass Daniel M, Folz-Donahue Kat, MacDonald Marcy E, Haggarty Stephen J
Chemical Neurobiology Laboratory, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts.
Center for Human Genetic Research, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts.
Curr Protoc Hum Genet. 2017 Jan 11;92:21.8.1-21.8.21. doi: 10.1002/cphg.33.
Reprogramming of human somatic cells into induced pluripotent stem (iPS) cells has greatly expanded the set of research tools available to investigate the molecular and cellular mechanisms underlying central nervous system (CNS) disorders. Realizing the promise of iPS cell technology for the identification of novel therapeutic targets and for high-throughput drug screening requires implementation of methods for the large-scale production of defined CNS cell types. Here we describe a protocol for generating stable, highly expandable, iPS cell-derived CNS neural progenitor cells (NPC) using multi-dimensional fluorescence activated cell sorting (FACS) to purify NPC defined by cell surface markers. In addition, we describe a rapid, efficient, and reproducible method for generating excitatory cortical-like neurons from these NPC through inducible expression of the pro-neural transcription factor Neurogenin 2 (iNgn2-NPC). Finally, we describe methodology for the use of iNgn2-NPC for probing human neuroplasticity and mechanisms underlying CNS disorders using high-content, single-cell-level automated microscopy assays. © 2017 by John Wiley & Sons, Inc.
将人类体细胞重编程为诱导多能干细胞(iPS细胞)极大地扩展了用于研究中枢神经系统(CNS)疾病潜在分子和细胞机制的研究工具集。要实现iPS细胞技术在鉴定新型治疗靶点和高通量药物筛选方面的前景,需要实施大规模生产特定CNS细胞类型的方法。在此,我们描述了一种使用多维荧光激活细胞分选(FACS)来纯化由细胞表面标志物定义的NPC,从而生成稳定、高度可扩增的iPS细胞来源的CNS神经祖细胞(NPC)的方案。此外,我们描述了一种通过诱导表达神经前体转录因子Neurogenin 2(iNgn2-NPC)从这些NPC生成兴奋性皮质样神经元的快速、高效且可重复的方法。最后,我们描述了使用iNgn2-NPC通过高内涵、单细胞水平自动显微镜检测来探究人类神经可塑性和CNS疾病潜在机制的方法。© 2017约翰威立国际出版公司